Don’t make medical device product labeling an afterthought

This webinar discusses how the recent EU MDR compliance deadline extension provides medical device manufacturers an opportunity to properly implement labeling and artwork solutions to mitigate risk of shortages and recalls.

It advises taking advantage of the extension to automate, optimize and centralize labeling to enable fast, flexible label changes and integrate with sources of truth.

The webinar also covers ensuring compliance through security, auditability and more. Tune in now to learn how to mitigate risk during the extension, ensure compliance, and avoid recalls.

Vendor:: Loftware
Premiered:: Apr 3, 2024
Format:: HTML
Type:: Webcast

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